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帕金森病患者中α-突触核蛋白()基因多态性与自发脑活动的关联。 (注:原文括号里内容缺失,翻译时保留原样)

Association of synuclein alpha () gene polymorphisms with spontaneous brain activity in patients with Parkinson's disease.

作者信息

Chen Fengxian, Chen Lina, Cai Guoen, Wang Yingqing, Li Yunjing, Xu Haoling, Song Wenjing, Jian Jing, Chen Xiaochun, Ye Qinyong

机构信息

Department of Neurology, Fujian Institute of Geriatrics, Fujian Medical University Union Hospital, Fuzhou, China.

Department of Neurology, The Second Affiliated Hospital of Xiamen Medical College, Xiamen, China.

出版信息

Quant Imaging Med Surg. 2024 Sep 1;14(9):6806-6819. doi: 10.21037/qims-24-14. Epub 2024 Aug 28.

Abstract

BACKGROUND

The synuclein alpha () gene responsible for encoding alpha-synuclein, is believed to play a crucial role in the pathogenesis of Parkinson's disease (PD). However, the specific impact of gene single-nucleotide polymorphisms (SNPs) on brain function in PD remains unclear. Therefore, this cross-sectional retrospective study, particularly through use of imaging analysis, aimed to characterize the relationship between gene SNPs and spontaneous brain activity in PD in order to enhance our understanding of the mechanisms underlying PD pathogenesis.

METHODS

A total of 63 patients with PD and 73 sex- and age-matched healthy control (HC) participants were recruited from outpatient and inpatient clinics at Fujian Medical University Union Hospital from August 2017 to November 2019, and all underwent a resting-state functional magnetic resonance imaging (rs-fMRI) scanning. All participants were also examined to determine the correlation of different genotypes with regional brain activity measured by rs-fMRI using amplitude of low-frequency fluctuation (ALFF) analysis. Multivariate regression analysis was used to calculate the correlation between the brain function data and clinical features. All rs-fMRI data were analyzed with the SPM12 software and adjusted according to the false discovery rate (FDR) at the cluster level.

RESULTS

This study included 63 patients with PD and 73 sex- and age-matched healthy participants were included in the study. The spontaneous brain activity in the right superior cerebellum (Cerebelum_Crus1_R), vermis (Vermis_7), and left supplementary motor area (Supp_Motor_Area_L) of patients in the PD group was weak compared to that in the HC group. The z-score ALFF of left central posterior gyrus was positively correlated with the Mini-Mental State Examination score (r=0.542; P<0.001) in the PD group. For rs11931074, the main genotypic effects were found in the left inferior cerebellum (Cerebellum_9_L) and right anterior cingulate and paracingulate gyri (Cingulum_Ant_R); for rs356219 and rs356165, the main genotypic effects were found in the left caudate nucleus (Caudate_L). An interaction effect of disease with genotype was found in the right inferior parietal gyrus (Parietal_Inf_R) only for rs356219.

CONCLUSIONS

Our study found a correlation of the SNPs rs11931074, rs356219, and rs356165 with brain functional alterations in patients with PD. Furthermore, an interaction effect was found in the right inferior parietal gyrus only for rs356219. This study may contribute to furthering the understanding of the influence of gene SNPs on brain function in patients with PD.

摘要

背景

负责编码α-突触核蛋白的突触核蛋白α()基因被认为在帕金森病(PD)的发病机制中起关键作用。然而,该基因单核苷酸多态性(SNP)对PD患者脑功能的具体影响仍不清楚。因此,这项横断面回顾性研究,特别是通过影像学分析,旨在描述该基因SNP与PD患者自发脑活动之间的关系,以增进我们对PD发病机制潜在机制的理解。

方法

2017年8月至2019年11月,从福建医科大学附属协和医院门诊和住院部招募了63例PD患者和73例性别和年龄匹配的健康对照(HC)参与者,所有参与者均接受静息态功能磁共振成像(rs-fMRI)扫描。所有参与者还接受检查,以确定不同基因型与使用低频振幅(ALFF)分析通过rs-fMRI测量的脑区活动之间的相关性。使用多元回归分析计算脑功能数据与临床特征之间的相关性。所有rs-fMRI数据均使用SPM12软件进行分析,并根据聚类水平的错误发现率(FDR)进行调整。

结果

本研究纳入了63例PD患者和73例性别和年龄匹配的健康参与者。与HC组相比,PD组患者右侧上小脑(Cerebelum_Crus1_R)、蚓部(Vermis_7)和左侧辅助运动区(Supp_Motor_Area_L)的自发脑活动较弱。PD组左侧中央后回的z-score ALFF与简易精神状态检查评分呈正相关(r = 0.542;P < 0.001)。对于rs11931074,主要基因型效应出现在左侧下小脑(Cerebellum_9_L)以及右侧前扣带回和旁扣带回(Cingulum_Ant_R);对于rs356219和rs356165,主要基因型效应出现在左侧尾状核(Caudate_L)。仅对于rs356219,在右侧顶下小叶(Parietal_Inf_R)发现疾病与基因型之间存在交互作用效应。

结论

我们的研究发现,该基因的SNP rs11931074、rs356219和rs356165与PD患者的脑功能改变相关。此外,仅对于rs356219,在右侧顶下小叶发现了交互作用效应。本研究可能有助于进一步了解该基因SNP对PD患者脑功能的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a8e/11400684/fbfb6e8f6bf5/qims-14-09-6806-f1.jpg

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